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230313001: Autosomal dominant late onset basal ganglia degeneration (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345139014 Autosomal dominant late onset basal ganglia degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618103016 Autosomal dominant late onset basal ganglia degeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
345139014 Autosomal dominant late onset basal ganglia degeneration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
345139014 Autosomal dominant late onset basal ganglia degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618103016 Autosomal dominant late onset basal ganglia degeneration (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
618103016 Autosomal dominant late onset basal ganglia degeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4958081000241117 dégénérescence autosomique dominante tardive des ganglions de base fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4958081000241117 dégénérescence autosomique dominante tardive des ganglions de base fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant late onset basal ganglia degeneration (disorder) Is a Basal ganglia degeneration with calcification (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant late onset basal ganglia degeneration (disorder) Finding site Basal ganglion structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant late onset basal ganglia degeneration (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant late onset basal ganglia degeneration (disorder) Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant late onset basal ganglia degeneration (disorder) Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant late onset basal ganglia degeneration (disorder) Associated morphology Pathologic calcification true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant late onset basal ganglia degeneration (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant late onset basal ganglia degeneration (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant late onset basal ganglia degeneration (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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